SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

Lignende værker

• Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance
  af: E. S. Naumova, et al.
  Udgivet: (2016-07-01)
• Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance
  af: E. S. Naumova, et al.
  Udgivet: (2016-07-01)
• Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis
  af: Kilfoyle, D H, et al.
  Udgivet: (2006)
• Hereditary Sensory and Autonomic Neuropathy Type IC with SPTLC2 Mutation Associated with Immune Thrombocytopenia
  af: Mansoor C. Abdulla
  Udgivet: (2022-07-01)
• Transcriptomic Analyses of Genes and Tissues in Inherited Sensory Neuropathies
  af: Sapio, Matthew R., et al.
  Udgivet: (2016)